Canonical Allele Identifier: PA111095
Gene: GGCX HGNC NCBI
ClinVar RCV:
RCV000017579
ClinVar Variation:
16195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000812.2:p.Trp501Ser
CA126263
NM_000821.7:c.1502G>C